Chiba Yoshihiko, Murata Masahiko, Ushikubo Hiroko, Yoshikawa Yuji, Saitoh Akiyoshi, Sakai Hiroyasu, Kamei Junzo, Misawa Miwa
Department of Pharmacology, School of Pharmacy, Hoshi University, 2-4-41 Ebara, Shinagawa-ku, Tokyo 142-8501, Japan.
Am J Respir Cell Mol Biol. 2005 Dec;33(6):574-81. doi: 10.1165/rcmb.2005-0177OC. Epub 2005 Sep 15.
Cigarette smoking is a risk factor for the development of airway hyperresponsiveness and chronic obstructive pulmonary disease. Little is known concerning the effect of cigarette smoking on the contractility of airway smooth muscle. The current study was performed to determine the responsiveness of bronchial smooth muscles isolated from rats that were subacutely exposed to mainstream cigarette smoke in vivo. Male Wistar rats were exposed to diluted mainstream cigarette smoke for 2 h/d every day for 2 wk. Twenty-four hours after the last cigarette smoke exposure, a marked airway inflammation (i.e., increases in numbers of neutrophils, lymphocytes, and macrophages in bronchoalveolar lavage fluid and peribronchial tissues) was observed. In these subacutely cigarette smoke-exposed animals, the responsiveness of isolated intact (nonpermeabilized) bronchial smooth muscle to acetylcholine, but not to high K+ -depolarization, was significantly augmented when compared with the air-exposed control group. In alpha-toxin-permeabilized bronchial smooth muscle strips, the acetylcholine-induced Ca2+ sensitization of contraction was significantly augmented in rats exposed to cigarette smoke, although the contraction induced by Ca2+ was control level. Immunoblot analyses revealed an increased expression of RhoA protein in the bronchial smooth muscle of rats that were exposed to cigarette smoke. Taken together, these findings suggest that the augmented agonist-induced, RhoA-mediated Ca2+ sensitization may be responsible for the enhanced bronchial smooth muscle contraction induced by cigarette smoking, which has relevance to airway hyperresponsiveness in patients with chronic obstructive pulmonary disease.
吸烟是气道高反应性和慢性阻塞性肺疾病发生的危险因素。关于吸烟对气道平滑肌收缩性的影响,目前所知甚少。本研究旨在确定从体内亚急性暴露于主流香烟烟雾的大鼠分离出的支气管平滑肌的反应性。雄性Wistar大鼠每天暴露于稀释的主流香烟烟雾中2小时,持续2周。在最后一次香烟烟雾暴露24小时后,观察到明显的气道炎症(即支气管肺泡灌洗液和支气管周围组织中中性粒细胞、淋巴细胞和巨噬细胞数量增加)。在这些亚急性暴露于香烟烟雾的动物中,与空气暴露对照组相比,分离的完整(未通透)支气管平滑肌对乙酰胆碱的反应性显著增强,但对高钾去极化的反应性未增强。在α-毒素通透的支气管平滑肌条中,尽管钙离子诱导的收缩处于对照水平,但香烟烟雾暴露大鼠中乙酰胆碱诱导的收缩钙离子敏化作用显著增强。免疫印迹分析显示,暴露于香烟烟雾的大鼠支气管平滑肌中RhoA蛋白表达增加。综上所述,这些发现表明,增强的激动剂诱导的、RhoA介导的钙离子敏化作用可能是吸烟诱导支气管平滑肌收缩增强的原因,这与慢性阻塞性肺疾病患者的气道高反应性有关。